XRCC4 Polyclonal Antibody, 20ul Drug Development and Evaluation Mutations in TUFM have been

Mutations in TUFM have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy

and thus represents a receptor-type PTP

This liquid medium is designed for optimal growth and productivity of CHO cells

a member of the thyroid-steroid hormone receptor superfamily of nuclear transcriptional regulators

ephrin-A2 (ELF-1) has been described as the ligand for EphA4

XRCC4 Polyclonal Antibody, 20ul Drug Development and Evaluation Mutations in TUFM have beenDNA repair protein XRCC4 encoded by XRCC4 functions together with DNA ligase IV and the DNA dependent protein kinase in the repair of DNA double strand breaks. This protein plays a role in both non homologous end joining and the completion of V(D)J recombination. Mutations in this gene can cause short stature, microcephaly, and endocrine dysfunction (SSMED). Alternative splicing generates several transcript variants.